Haidong Fu

Fluid management of hypernatraemic dehydration to prevent cerebral oedema: a retrospective case control study of 97 children in China.

Clinical outcomes in children with Henoch-Schönlein purpura nephritis grade IIIa or IIIb.

Treatment of tacrolimus or cyclosporine A in children with idiopathic nephrotic syndrome.

Rituximab followed by mycophenolate mofetil in children with IgM nephropathy.

Persistent asymptomatic isolated hematuria in children: clinical and histopathological features and prognosis.

[Acute kidney injury induced by favism in children: a case report].

Overexpression of Myo1e in mouse podocytes enhances cellular endocytosis, migration, and adhesion.

Efficacy of triptolide for children with moderately severe Henoch-Schönlein purpura nephritis presenting with nephrotic range proteinuria: a prospective and controlled study in China.

Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review.

Interferon-gamma gene polymorphism +874 (a/t) in Chinese children with Henoch-Schonlein purpura.

Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children.

Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing.

Clinical characteristics of concomitant nephrotic IgA nephropathy and minimal change disease in children.

Evaluation of mycophenolate mofetil or tacrolimus in children with steroid sensitive but frequently relapsing or steroid-dependent nephrotic syndrome.

The Value of Monitoring the Serum Concentration of Mycophenolate Mofetil in Children with Steroid-Dependent/Frequent Relapsing Nephrotic Syndrome.

Association between IL17A and IL17F polymorphisms and risk of Henoch-Schonlein purpura in Chinese children.

Huaiqihuang may protect from proteinuria by resisting MPC5 podocyte damage via targeting p-ERK/CHOP pathway.

Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.

Clinical features and outcomes of diffuse endocapillary proliferation Henoch-Schönlein purpura nephritis in children.

Beneficial effects of Huaiqihuang on hyperglycemia-induced MPC5 podocyte dysfunction through the suppression of mitochondrial dysfunction and endoplasmic reticulum stress.

Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review.

Analysis of 17 children with renal abscess.

Clinical features and genetic findings in Chinese children with distal renal tubular acidosis.

Overexpression of Myo1e promotes albumin endocytosis by mouse glomerular podocytes mediated by Dynamin.

Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).

Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review.

Clinical and genetic characteristics of concomitant Mucopolysaccharidosis type IVA and neurogenic bladder in children: two case reports and literature review.

Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1.

Roxadustat for Renal Anemia in ESRD from PKD Patients: Is It Safe Enough?

Case Report: Membranoproliferative Glomerulonephritis, a Rare Clinical Manifestation of Abernethy Malformation Type II.

Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.

Activated phosphoinositide 3-kinase delta syndrome misdiagnosed as anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report.

The immune cell landscape of peripheral blood mononuclear cells from PNS patients.

Renoprotection with sodium-glucose cotransporter-2 inhibitors in children: Knowns and unknowns.

Establishment of an induced pluripotent stem cell line (NCKDi003-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p. T277P (c. 829A > C) in the CLCN5 gene.

Coronavirus disease 2019 vaccine for children in China: when to start? Mandatory or voluntary?

Seven novel podocyte autoantibodies were identified to diagnosis a new disease subgroup-autoimmune Podocytopathies.

PP2A protects podocytes against Adriamycin-induced injury and epithelial-to-mesenchymal transition via suppressing JIP4/p38-MAPK pathway.

Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report.

New-onset and relapsing glomerular diseases related to COVID-19 vaccination.

Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study.

The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome.

Urinary Sediment mRNA Level of CREBBP and CYBA in Children With Steroid-Resistant Nephrotic Syndrome.

Renoprotective Role of Hypoxia-Inducible Factors and the Mechanism.

Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome.

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.

Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients.

Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with Mutations.

Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.

Vasculitis after COVID-19 Vaccination.

The interaction between cellular senescence and chronic kidney disease as a therapeutic opportunity.

Psychological research of the children with chronic kidney disease and their guardians during the COVID-19 pandemic.

Glomerular diseases after immune checkpoint inhibitors use: What do We know so far?

COVID-19 Breakthrough Infections in Vaccinated Kidney Transplant Recipients.

Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy.

Benefits and risks of essential trace elements in chronic kidney disease: a narrative review.

Advances in imaging techniques to assess kidney fibrosis.

Roxadustat: Do we know all the answers?

Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome.

A quantitative planar array screen of 440 proteins uncovers novel serum protein biomarkers of idiopathic nephrotic syndrome.